A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526713



Internal ID15107320
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5527507..5552407hg38UCSC Ensembl
Innerchr4:5529234..5554134hg19UCSC Ensembl
Innerchr4:5580135..5605035hg18UCSC Ensembl
Innerchr4:5647306..5672206hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3824901
hg1924901
hg1824901
hg1724901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703053
Samples
Known GenesC4orf6
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526713
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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